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Clinical Trials in Turkey / NCT07683559
Starting soon Not applicable

Extracorporeal Shock Wave Therapy in Patients With Lipedema

NCT07683559 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2026-07-01
Last updated
2026-07-06

Condition(s) studied

Lipedema

Investigational drug(s) / intervention(s)

Extracorporeal Shock Wave Therapy

Extracorporeal Shock Wave Therapy: Extracorporeal shock wave therapy (ESWT) will be applied to affected lower-extremity regions using a CE-marked shock wave device. Participants will receive six treatment sessions administered three times per week for two consecutive weeks. Clinical and ultrasonographic assessments will be performed before and after treatment.

Study summary

Lipedema is a chronic adipose tissue disorder characterized by pain, tenderness, disproportionate fat accumulation, and impaired quality of life. Extracorporeal shock wave therapy (ESWT) has been proposed as a non-invasive treatment option that may improve pain and tissue characteristics in patients with lipedema.

The aim of this prospective interventional study is to evaluate the effects of ESWT on pain intensity, quality of life, functional outcomes, and ultrasonographic findings in patients diagnosed with lipedema. Participants will receive a standardized ESWT protocol consisting of six treatment sessions over a two-week period. Clinical assessments and ultrasonographic examinations will be performed before and after treatment.

Eligibility

Sex
ALL
Min age
18 Years
Max age
75 Years
Healthy volunteers
No
Inclusion Criteria: * Male or female participants aged 18 to 75 years * Clinical diagnosis of lipedema * Willingness to participate and provide written informed consent * Ability to comply with study procedures and follow-up assessments Exclusion Criteria: * Pregnancy or breastfeeding * Active infection in the treatment area * Malignancy * Severe cardiovascular disease * Coagulation disorders or current anticoagulant therapy * Previous ESWT treatment within the last 6 months * Severe psychiatric or cognitive disorders interfering with study participation * Any condition deemed by the investigator to make participation unsafe

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Kanuni Sultan Suleyman Training and Research Hospital Istanbul Istanbul

More Atlas University trials in Turkey

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07683559 on ClinicalTrials.gov ↗ ← All trials in Turkey